45 articles for MI Choudhary
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Cmpds
Data
Article Title
Organization
23
Xanthine oxidase inhibitory activity of nicotino/isonicotinohydrazides: A systematic approach from in vitro, in silico to in vivo studies.
University of Karachi
25
Synthesis of diethyl 4-substituted-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylates as a new series of inhibitors against yeasta-glucosidase.
University of Karachi
26
Synthesis of novel inhibitors ofa-glucosidase based on the benzothiazole skeleton containing benzohydrazide moiety and their molecular docking studies.
Universiti Teknologi Mara (Uitm)
5
Substituted thieno[2,3-b]thiophenes and related congeners: Synthesis,ß-glucuronidase inhibition activity, crystal structure, and POM analyses.
King Saud University
26
Synthesis andß-glucuronidase inhibitory activity of 2-arylquinazolin-4(3H)-ones.
University of Karachi
11
Evaluation of bisindole as potentß-glucuronidase inhibitors: synthesis and in silico based studies.
University of Karachi
37
Synthesis and in vitro urease inhibitory activity of N,N'-disubstituted thioureas.
University Karachi
5
Fungal transformation of cedryl acetate anda-glucosidase inhibition assay, quantum mechanical calculations and molecular docking studies of its metabolites.
University of Karachi
30
3D-QSAR CoMFA studies on bis-coumarine analogues as urease inhibitors: a strategic design in anti-urease agents.
University of Karachi
30
3D-QSAR studies on natural acetylcholinesterase inhibitors of Sarcococca saligna by comparative molecular field analysis (CoMFA).
University of Innsbruck
5
Isoflavone dimers and other bioactive constituents from the figs of Ficus mucuso.
University of Yaounde
10
New class of acetylcholinesterase inhibitors from the stem bark of Knema laurina and their structural insights.
University Putra Malaysia
10
Synthesis, antioxidant activities and urease inhibition of some new 1,2,4-triazole and 1,3,4-thiadiazole derivatives.
Quaid-I-Azam University
8
1,3,4-Oxadiazole-2(3H)-thione and its analogues: a new class of non-competitive nucleotide pyrophosphatases/phosphodiesterases 1 inhibitors.
University of Karachi
7
Bioactive 5alpha-pregnane-type steroidal alkaloids from Sarcococca hookeriana.
Bielefeld University
11
Microbial transformation and butyrylcholinesterase inhibitory activity of (-)-caryophyllene oxide and its derivatives.
University of Karachi
4
New triterpenoid alkaloid cholinesterase inhibitors from Buxus hyrcana.
University of Karachi
3
Steroidal alkaloids from the leaves of Sarcococca coriacea of Nepalese origin.
Tribhuvan University
10
Isolation and cholinesterase-inhibition studies of sterols from Haloxylon recurvum.
University of Karachi
13
Microwave-Assisted Organic Synthesis, structure-activity relationship, kinetics and molecular docking studies of non-cytotoxic benzamide derivatives as selective butyrylcholinesterase inhibitors.
University of Karachi
13
Schiff bases of 3-formylchromone as thymidine phosphorylase inhibitors.
University of Karachi
3
Biotransformation of (-)-ambrox by cell suspension cultures of Actinidia deliciosa.
University of Karachi
150
Pyridone derivative, pharmaceutical containing the same and methods of use thereof
Kaken Pharmaceutical
28
Non-peptide macrocyclic histone deacetylese (HDAC) inhibitors and methods of making and using thereof
Georgia Tech Research
13
Synthesis, molecular docking, and biological evaluation of some novel hydrazones and pyrazole derivatives as anti-inflammatory agents.
Cairo University
29
Pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use
F. Hoffmann-La Roche
5
PIF-pocket as a target for C. albicans Pkh selective inhibitors.
Universit£Tsklinikum Frankfurt
5
Non-amidic linkers with branched termini as CGRP receptor antagonists
Merck Sharp & Dohme
15
Synthesis and biological evaluation of thienopyrrolizines, a new family of CDK/GSK-3 inhibitors.
UniversitÉ
4
Behaviroal, pharmacological, and molecular characterization of an amphibian cannabinoid receptor.
Oregon State University
22
Characterization and function of the bovine kidney epithelial angiotensin receptor subtype 4 using angiotensin IV and divalinal angiotensin IV as receptor ligands.
Washington State University
1
6-Methyl-3'-bromoflavone, a high-affinity ligand for the benzodiazepine binding site of the GABA(A) receptor with some antagonistic properties.
Instituto De BiologÍA Celular
16
7-Chloro-5-hydroxy-1-[2-methyl-4-(2-methylbenzoyl-amino)benzoyl ]-2,3,4,5-tetrahydro-1H-1-benzazepine (OPC-41061): a potent, orally active nonpeptide arginine vasopressin V2 receptor antagonist.
Otsuka Pharmaceutical